Malignant hyperthermia in Lesch-Nyhan disease
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Peertechz Publications Private Limited
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https://www.peertechzpublications.com/articles/ACN-5-134.pdf
Reference7 articles.
1. 1. Lesch M, Nyhan WL (1964) A familial disorder of uric acid metabolism and central nervous system function. Am J Med 36: 561-570. Link: https://tinyurl.com/y56tmdpd
2. 2. Seegmiller JE, Rosenbloom FM, Kelley WN (1967) Enzyme defect associated with sex-linked human neurological disorder and excessive purine synthesis. Science 155: 1682-1684. Link: https://tinyurl.com/y2vtx27a
3. 3. Jolly DL, Esty AC, Bernard HU, Friedman T (982) Isolation f an genomic clone encoding human hypoxanthine guanine phosphoribosyl transferase. Proc Natl Acad Sci USA 79: 5038-5041. Link: https://tinyurl.com/y2cbspbo
4. 4. Jolly DL, Okayama H, Berg P (1983) Isolation and characterization of a full length, expressible cDNA for human hypoxanthine guanine phosphoribosyl transferase. Proc Natl Acad Sci USA 80: 477-841. Link: https://tinyurl.com/y4nq5mna
5. 5. Jinnah HA, De Gregorio L, Harris JC (2000) The spectrum of inherited mutations causing HPRT deficiency: 75 new cases and a review of 196 previously reported cases. Mutat Res 463: 309-326. Link: https://tinyurl.com/y4lv5dx7
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